Schnoy N, Bein G, Dumke K
Monatsschr Kinderheilkd (1902). 1978 Jul;126(7):431-5.
We report the clinical and post-mortem findings of an infant with inborn short bowel. One sibling died because of the same malformation. The parents are cousins. This malformation is combined with malrotation, often with pylorus-stenosis too, and can cause an intestinal obstruction syndrome. All presently known cases in the pertinent literature are summarized. The occurence of familial cases suggest a rezessive autosomal disease.
我们报告了一名患有先天性短肠婴儿的临床和尸检结果。其一名同胞因同样的畸形死亡。父母是近亲。这种畸形常合并肠旋转不良，也常伴有幽门狭窄，可导致肠梗阻综合征。本文总结了相关文献中目前已知的所有病例。家族性病例的出现提示为常染色体隐性疾病。
